US2013226307A1PendingUtilityA1

Coated endoprostheses and related systems & methods

Assignee: AMEDICA CORPPriority: Feb 28, 2012Filed: Feb 27, 2013Published: Aug 29, 2013
Est. expiryFeb 28, 2032(~5.6 yrs left)· nominal 20-yr term from priority
A61F 2/3094A61F 2310/00317A61L 27/306A61L 27/303A61F 2310/0058A61L 27/10A61F 2310/00682A61F 2310/00742A61F 2310/0088A61F 2/3601A61F 2/32
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Claims

Abstract

Methods for performing a hemiarthroplasty procedure. In some implementations, the method may comprise providing a component of an endoprosthesis, such as a femoral component of a hip prosthesis. The component may comprise a silicon nitride ceramic material, and may further comprise a coated articulating surface. The coated articulating surface may comprise a coating configured to reduce a coefficient of friction of the articulating surface. The method may further comprise positioning the endoprosthesis such that the coated articulating surface is positioned adjacent to a patient's native articular cartilage. In this manner, the coated articulating surface may articulate with the native articular cartilage following the procedure.

Claims

exact text as granted — not AI-modified
1 . A method for performing a hemiarthroplasty procedure, the method comprising the steps of:
 providing a component of an endoprosthesis, wherein the component comprises a silicon nitride ceramic material, and wherein the component further comprises a coated articulating surface comprising a coating, wherein the coating comprises at least one of diamond-like carbon, silicon carbide, titanium nitride, titanium diboride, titanium carbonitride, titanium aluminum nitride, chromium nitride, chromium carbonitride, and titanium silicon carbonitride; and   positioning the endoprosthesis such that the coated articulating surface is positioned adjacent to a patient's native articular cartilage such that the coated articulating surface is configured to articulate with the native articular cartilage following the procedure.   
     
     
         2 . The method of  claim 1 , wherein the silicon nitride ceramic material comprises a doped silicon nitride ceramic material. 
     
     
         3 . The method of  claim 2 , wherein the doped silicon nitride ceramic material comprises dopants selected from the group consisting of yttrium oxide, magnesium oxide, strontium oxide, aluminum oxide, and combinations thereof. 
     
     
         4 . The method of  claim 1 , wherein the native articular cartilage comprises articular cartilage in the patient's acetabulum. 
     
     
         5 . The method of  claim 1 , wherein the coated articulating surface has a coefficient of friction of between about 0.008 and about 0.03. 
     
     
         6 . The method of  claim 5 , wherein the coated articulating surface has a coefficient of friction of between about 0.009 and about 0.02. 
     
     
         7 . The method of  claim 6 , wherein the coated articulating surface has a coefficient of friction of about 0.01. 
     
     
         8 . The method of  claim 1 , wherein the component further comprises an uncoated surface. 
     
     
         9 . A method for applying a coating to an articulating surface of an endoprosthesis, the method comprising the steps of:
 providing a component of an endoprosthesis, wherein the component comprises an articulating surface, wherein the articulating surface is configured to interface with a patient's native articular cartilage, and wherein the component comprises a silicon nitride ceramic material;   applying a coating to the articulating surface, wherein the coating comprises at least one of diamond-like carbon, silicon carbide, titanium nitride, titanium diboride, titanium carbonitride, titanium aluminum nitride, chromium nitride, chromium carbonitride, and titanium silicon carbonitride.   
     
     
         10 . The method of  claim 9 , wherein the silicon nitride ceramic material comprises a doped silicon nitride ceramic material. 
     
     
         11 . The method of  claim 10 , wherein the doped silicon nitride ceramic material comprises dopants selected from the group consisting of yttrium oxide, magnesium oxide, strontium oxide, aluminum oxide, and combinations thereof. 
     
     
         12 . The method of  claim 9 , wherein the component comprises a femoral component, and wherein the articulating surface comprises a surface of a ball-shaped head of the femoral component. 
     
     
         13 . The method of  claim 9 , wherein the step of applying a coating to the articulating surface comprises applying the coating using at least one of a physical vapor deposition and a chemical vapor deposition process. 
     
     
         14 . The method of  claim 9 , wherein the step of applying a coating to the articulating surface comprises applying a diamond-like carbon material to the articulating surface. 
     
     
         15 . The method of  claim 14 , wherein the step of applying a coating to the articulating surface comprises applying a diamond-like carbon material to the articulating surface using a physical vapor deposition process. 
     
     
         16 . The method of  claim 9 , wherein the step of applying a coating to the articulating surface reduces the coefficient of friction of the articulating surface from between about 0.1 and about 0.4 to between about 0.005 and about 0.05. 
     
     
         17 . The method of  claim 9 , wherein the step of applying a coating to the articulating surface reduces the coefficient of friction of the articulating surface to between about 0.008 and about 0.03. 
     
     
         18 . The method of  claim 17 , wherein the step of applying a coating to the articulating surface reduces the coefficient of friction of the articulating surface to between about 0.009 and about 0.02. 
     
     
         19 . The method of  claim 18 , wherein the step of applying a coating to the articulating surface reduces the coefficient of friction of the articulating surface to about 0.01. 
     
     
         20 . A method for performing a hip hemiarthroplasty procedure, the method comprising the steps of:
 providing a femoral component comprising a femoral head and a stem, wherein the stem is configured to be coupled with an upper end of a patient's femur, wherein the femoral component comprises a doped silicon nitride ceramic material comprising dopants selected from the group consisting of yttrium oxide, magnesium oxide, strontium oxide, aluminum oxide, and combinations thereof, wherein the femoral head comprises a coated articulating surface comprising a coating, wherein the coating comprises at least one of diamond-like carbon, silicon carbide, titanium nitride, titanium diboride, titanium carbonitride, titanium aluminum nitride, chromium nitride, chromium carbonitride, and titanium silicon carbonitride, wherein the coated articulating surface has a coefficient of friction of no more than about 0.01, and wherein the femoral component other than the coated articulating surface has a coefficient of friction of at least about 0.1; and   positioning the femoral component such that the coated articulating surface is positioned adjacent to a patient's native articular cartilage within the patient's acetabulum such that the coated articulating surface is configured to articulate with the native articular cartilage following the procedure.

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